510(k) Report

FDA applicant

Selicor, Inc.

San Antonio, TX2 decisions2002–20030 recalls

FDA records 2 decisions for Selicor, Inc. (San Antonio, TX) from 2002 to 2003: 2 510(k) clearances. All are in product code IMJ (Diathermy, Shortwave, For Use In Applying…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Selicor, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Selicor, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Selicor, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IMJDiathermy, Shortwave, For Use In Applying Therapeutic Deep Heat2decisions

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K030382Selitherm, Model C100Selicor, Inc. · 20031cites it

What has FDA decided for it lately?

  • K030382Selitherm, Model C100Selicor, Inc. · 2003
  • K020227Selicor, Models A100 & D100Selicor, Inc. · 2002

All 2 as Selicor, Inc. →